DK57181A - PROCEDURE FOR THE PREPARATION OF 4-SUBSTITUTED IMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS. - Google Patents

PROCEDURE FOR THE PREPARATION OF 4-SUBSTITUTED IMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS.

Info

Publication number
DK57181A
DK57181A DK57181A DK57181A DK57181A DK 57181 A DK57181 A DK 57181A DK 57181 A DK57181 A DK 57181A DK 57181 A DK57181 A DK 57181A DK 57181 A DK57181 A DK 57181A
Authority
DK
Denmark
Prior art keywords
sub
acid addition
addition salts
compounds
acceptable acid
Prior art date
Application number
DK57181A
Other languages
Danish (da)
Other versions
DK157861B (en
DK157861C (en
Inventor
A J Karjalainen
K O A Kurkela
Original Assignee
Farmos Oy
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Farmos Oy filed Critical Farmos Oy
Publication of DK57181A publication Critical patent/DK57181A/en
Publication of DK157861B publication Critical patent/DK157861B/en
Application granted granted Critical
Publication of DK157861C publication Critical patent/DK157861C/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10—Antioedematous agents; Diuretics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Catalysts (AREA)

Abstract

The invention provides compounds of the formula:wherein each of R<sub>1</sub>, R<sub>2</sub> and R<sub>3</sub>, which can be the same or different is hydrogen, chloro, bromo, fluoro, methyl, ethyl, methoxv, amino, hydroxy or nitro; R<sub>4</sub> is hydrogen or alkyl of 1 to 7 carbon atoms; X is(R<sub>5</sub> is hydrogen or hydroxy) and n is 1-4; and their non-toxic pharmaceutically acceptable acid addition salts. These compounds exhibitvaluable pharmacological activity and are useful in the treatment of mammals, especially as anti- hypertensive agents. Furthermore, some of the compounds have proved to possess diuretic, ß-blocking activity and/or antithrombotic activity. The compounds may be made by a variety of methods and may be incorporated in pharmaceutical compositions also comprising a compatible pharmaceutically acceptable carrier.
DK057181A 1980-02-13 1981-02-11 METHOD OF ANALOGUE FOR THE PREPARATION OF 4-SUBSTITUTED PHENYLALKYLIMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS. DK157861C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8004748 1980-02-13
GB8004748A GB2069481B (en) 1980-02-13 1980-02-13 Substituted imidazole derivatives

Publications (3)

Publication Number Publication Date
DK57181A true DK57181A (en) 1981-08-14
DK157861B DK157861B (en) 1990-02-26
DK157861C DK157861C (en) 1990-07-30

Family

ID=10511309

Family Applications (2)

Application Number Title Priority Date Filing Date
DK057181A DK157861C (en) 1980-02-13 1981-02-11 METHOD OF ANALOGUE FOR THE PREPARATION OF 4-SUBSTITUTED PHENYLALKYLIMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS.
DK057281A DK151627C (en) 1980-02-13 1981-02-11 METHOD OF ANALOGUE FOR THE PREPARATION OF THERAPEUTIC ACTIVITY 4- (PHENYLALKENYL) IMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS.

Family Applications After (1)

Application Number Title Priority Date Filing Date
DK057281A DK151627C (en) 1980-02-13 1981-02-11 METHOD OF ANALOGUE FOR THE PREPARATION OF THERAPEUTIC ACTIVITY 4- (PHENYLALKENYL) IMIDAZOLD DERIVATIVES OR TOXIC PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALTS.

Country Status (17)

Country Link
US (3) US4333947A (en)
EP (2) EP0034474B1 (en)
JP (2) JPS56128767A (en)
AT (2) ATE2322T1 (en)
AU (2) AU537028B2 (en)
CA (2) CA1167454A (en)
DD (1) DD156260A1 (en)
DE (2) DE3160905D1 (en)
DK (2) DK157861C (en)
FI (2) FI73415C (en)
GB (1) GB2069481B (en)
IE (2) IE50771B1 (en)
IL (2) IL62110A (en)
NO (2) NO154089C (en)
NZ (2) NZ196251A (en)
SU (1) SU1074404A3 (en)
ZA (2) ZA81977B (en)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2092569B (en) * 1981-02-05 1984-09-19 Farmos Oy Substituted imidazole derivatives and their preparation and use
GB2101114B (en) * 1981-07-10 1985-05-22 Farmos Group Ltd Substituted imidazole derivatives and their preparation and use
ES535188A0 (en) * 1983-08-17 1985-12-01 Syntex Inc PROCEDURE FOR THE PREPARATION OF ALPHA-AMINO ACIDS ALPHA-ALENICOS
JPH062746B2 (en) * 1984-07-23 1994-01-12 三井石油化学工業株式会社 Method for producing imidazoles
LU85747A1 (en) * 1985-01-28 1986-08-04 Continental Pharma IMIDAZOLE DERIVATIVES, PREPARATION AND USE THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING DERIVATIVES
GB8523255D0 (en) * 1985-09-20 1985-10-23 Shell Int Research Imidazoles
DE3539629A1 (en) * 1985-11-08 1987-05-14 Basf Ag DIALKOXYKETONE AND A METHOD FOR THE PRODUCTION THEREOF
US4882343A (en) * 1987-08-28 1989-11-21 G. D. Searle & Co. Biarylalkylimidazole derivatives as anti-depressants
GB2210875B (en) * 1987-10-09 1991-05-29 Farmos Oy Aromatase inhibiting 4(5)-imidazoles
GB8726110D0 (en) * 1987-11-06 1987-12-09 Shell Int Research Imidazole ketone derivatives
US5354867A (en) * 1988-12-06 1994-10-11 E. I. Du Pont De Nemours And Company Angiotensin II receptor blocking imidazoles
US5304569A (en) * 1989-11-13 1994-04-19 Orion-Yhtyma Oy Compositions and their use in lowering intraocular pressure
DE4003243A1 (en) * 1990-02-03 1991-08-08 Basf Ag Use of tri:alkanolamine polyether(s) as demulsifiers in o/w emulsions - obtainable by condensing tri:alkanol:amine(s) in presence of (hypo)phosphorous acid
DE4006255A1 (en) * 1990-02-28 1991-08-29 Basf Ag CONDENSATION PRODUCTS SUITABLE AS EMULGATORS OF OIL-IN-WATER EMULSIONS
GB2256135B (en) 1991-05-31 1995-01-18 Orion Yhtymae Oy Transdermal administration of 4-substituted imidazoles
DE4136661A1 (en) * 1991-11-07 1993-05-13 Basf Ag PETROLEUM EMULSION SPLITTER
US5922751A (en) * 1994-06-24 1999-07-13 Euro-Celtique, S.A. Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same
FR2732017B1 (en) * 1995-03-21 2000-09-22 Inst Nat Sante Rech Med NOVEL IMIDAZOLE DERIVATIVES AND / OR HISTAMINE H3 RECEPTOR AGONISTS AND / OR AGONISTS, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATIONS
DK0841922T3 (en) * 1995-05-30 2002-06-03 Gliatech Inc 1H-4 (5) -substituted imidazole derivatives
JPH099441A (en) * 1995-06-21 1997-01-10 Yoshinari Denki Kogyosho:Kk Cable bender
WO2000039716A2 (en) * 1998-12-23 2000-07-06 Astrazeneca Ab Arylpropenylimidazoles as farnesyl-protein transferase inhibitors
BRPI0408136A (en) 2003-03-07 2006-03-01 Astellas Pharma Inc nitrogen-containing heterocyclic derivatives having 2,6-disubstituted styryl
EP1918282A1 (en) * 2006-11-06 2008-05-07 "Joint Stock Company Grindeks" Method for preparing medetomidine and its salts
US20080146523A1 (en) * 2006-12-18 2008-06-19 Guido Galley Imidazole derivatives
CN118715219A (en) * 2022-01-20 2024-09-27 瓦勒莱塞逊瑞彻弛Hscm有限合伙公司 Resolvinol analog compounds and methods and uses thereof

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2946804A (en) * 1958-12-29 1960-07-26 Abbott Lab (5-methyl-4-imidazolyl)-diphenyl carbinol salts and lower alkyl quaternaries
US3050520A (en) * 1960-03-31 1962-08-21 Air Prod & Chem Process of preparing 2-olefinic imidazoles
US3188315A (en) * 1960-05-18 1965-06-08 Schering Corp Novel compounds for lowering blood cholesterol levels
US3202660A (en) * 1961-10-09 1965-08-24 Boehringer Sohn Ingelheim Process for the preparation of 3-arylamino-1, 3-diazacycloalkenes
US3448108A (en) * 1965-04-16 1969-06-03 Schering Corp Substituted phenethyl heterocycles and their derivatives
US3502661A (en) * 1967-02-14 1970-03-24 Pfizer & Co C Process for making 1,4,5,6-tetrahydro-2-((2-substituted)vinyl) pyrimidines and 2-((2-substituted)vinyl)-2-imidazolines
BE793407A (en) * 1971-12-28 1973-06-28 Hoechst Ag IMIDAZOLYL - (2) -CARBINOLS HAVING HYPOLIPIDEMIC ACTIVITY AND THEIR PREPARATION PROCESS
US3812111A (en) * 1972-12-04 1974-05-21 Commercial Solvents Corp Imidazoline tranquilizing agents
IE40911B1 (en) * 1974-04-11 1979-09-12 Schering Ag Imidazole derivatives and process for their manufacture
US3991201A (en) * 1974-06-27 1976-11-09 Janssen Pharmaceutica N.V. 1-(β-Aryl-β-R-ethyl)imidazoles as antimicrobial agents
US4085209A (en) * 1975-02-05 1978-04-18 Rohm And Haas Company Preparation and safening effect of 1-substituted imidazole metal salt complexes
US4006137A (en) * 1975-08-21 1977-02-01 E. R. Squibb & Sons, Inc. 2-Ethenyl imidazolium derivatives
US4115578A (en) * 1975-12-18 1978-09-19 Rohm And Haas Company 1-Substituted aralkyl imidazoles
DE2862079D1 (en) * 1977-10-26 1982-12-09 Wellcome Found Imidazoline derivatives and salts thereof, their synthesis, pesticidal formulations containing the imidazolines, preparation thereof and their use as pesticides
GB2025934B (en) * 1978-06-22 1982-08-04 Grissmann Chem Ltd (1 - alkyl - 5 - nitro - 2 - imidozolyl)-vinylglyoxal-diacetals their preparation and their use
IT1097314B (en) * 1978-07-26 1985-08-31 Recordati Chem Pharm DERIVATIVES OF IMIDAZOLE WITH ANTI-CONVULSIVE ACTIVITY
DE2851116A1 (en) * 1978-11-25 1980-06-12 Bayer Ag HYDROXYETHYL AZOLE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A MEDICINAL PRODUCT
US4260626A (en) * 1979-03-26 1981-04-07 Richardson-Merrell Inc. Tetrahydro and imidazoline antisecretory compounds
AU518569B2 (en) * 1979-08-07 1981-10-08 Farmos-Yhtyma Oy 4-benzyl- and 4-benzoyl imidazole derivatives
GB2101114B (en) * 1981-07-10 1985-05-22 Farmos Group Ltd Substituted imidazole derivatives and their preparation and use

Also Published As

Publication number Publication date
DK151627B (en) 1987-12-21
JPS56128768A (en) 1981-10-08
NO153455C (en) 1986-05-07
US4333947A (en) 1982-06-08
FI810250L (en) 1981-08-14
GB2069481A (en) 1981-08-26
CA1160238A (en) 1984-01-10
IE810275L (en) 1981-08-13
GB2069481B (en) 1983-07-27
ATE2322T1 (en) 1983-02-15
AU6716381A (en) 1981-08-20
IL62110A (en) 1986-01-31
NO154089B (en) 1986-04-07
CA1167454A (en) 1984-05-15
NO810479L (en) 1981-08-14
DE3160905D1 (en) 1983-10-27
NO810478L (en) 1981-08-14
DK157861B (en) 1990-02-26
IL62111A (en) 1985-03-31
ATE4709T1 (en) 1983-10-15
NZ196250A (en) 1983-06-17
ZA81977B (en) 1982-03-31
DK151627C (en) 1988-06-20
FI810389L (en) 1981-08-14
NO153455B (en) 1985-12-16
AU537028B2 (en) 1984-05-31
EP0034473A2 (en) 1981-08-26
NO154089C (en) 1986-07-16
FI73415C (en) 1987-10-09
IE810274L (en) 1981-08-13
JPH0215538B2 (en) 1990-04-12
JPS56128767A (en) 1981-10-08
IE50772B1 (en) 1986-07-09
EP0034473A3 (en) 1981-11-18
DE3160036D1 (en) 1983-03-03
DD156260A1 (en) 1982-08-11
ZA81978B (en) 1982-03-31
AU528275B2 (en) 1983-04-21
FI73416C (en) 1987-10-09
FI73415B (en) 1987-06-30
DK57281A (en) 1981-08-14
AU6716481A (en) 1981-08-20
NZ196251A (en) 1983-05-31
EP0034474B1 (en) 1983-01-26
FI73416B (en) 1987-06-30
US4684659A (en) 1987-08-04
DK157861C (en) 1990-07-30
EP0034473B1 (en) 1983-09-21
US4568686A (en) 1986-02-04
IE50771B1 (en) 1986-07-09
EP0034474A1 (en) 1981-08-26
SU1074404A3 (en) 1984-02-15
JPH0249308B2 (en) 1990-10-29

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Legal Events

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PBP Patent lapsed